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NTLA-2002 in Adults With Hereditary Angioedema (HAE)
Sponsor: Intellia Therapeutics
Summary
This study will be conducted to evaluate the safety, tolerability, activity, pharmacokinetics, and pharmacodynamics of NTLA-2002 in adults with Hereditary Angioedema (HAE).
Official title: Phase 1/2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NTLA-2002 in Adults With Hereditary Angioedema (HAE)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
37
Start Date
2021-12-10
Completion Date
2026-07
Last Updated
2026-03-24
Healthy Volunteers
No
Conditions
Interventions
Biological NTLA-2002
CRISPR/Cas9 gene editing system delivered by LNP for IV administration
Normal Saline IV Administration
The administration of IV normal saline
Locations (9)
Clinical Trial Site
Campbelltown, Australia
Clinical Trial Site
Grenoble, France
Clinical Trial Site
Lille, France
Clinical Trial Site
Paris, France
Clinical Trial Site
Berlin, Germany
Clinical Trial Site
Frankfurt, Germany
Clinical Trial Site
Amsterdam, Netherlands
Clinical Trial Site
Auckland, New Zealand
Clinical Trial Site
Cambridge, United Kingdom